- Trials with a EudraCT protocol (7)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
7 result(s) found for: Toothache.
Displaying page 1 of 1.
EudraCT Number: 2005-005478-66 | Sponsor Protocol Number: PDY5808 | Start Date*: 2006-02-09 | |||||||||||
Sponsor Name:Sanofi-Synthelabo Recherche | |||||||||||||
Full Title: Effect of a single oral 120 µg dose of SSR150106XB compared to placebo on the assessment of post dental surgical pain after extraction of an impacted or partially impacted third molar in 90 male an... | |||||||||||||
Medical condition: Men and women who are to undergo elective surgery for extraction of at least one lower impacted or partially impacted third molar | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-003274-22 | Sponsor Protocol Number: 22093 | Start Date*: 2022-10-25 | ||||||||||||||||
Sponsor Name:Bayer HealthCare LLC | ||||||||||||||||||
Full Title: A Randomized, Double-Blind, Single-Dose, Parallel, Placebo-Controlled Pivotal Trial to Confirm the Efficacy of a Fixed Dose Combination Tablet of Naproxen Sodium and Caffeine to Effectively Allevia... | ||||||||||||||||||
Medical condition: Postoperative dental pain | ||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: Outside EU/EEA | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-001795-38 | Sponsor Protocol Number: A206 | Start Date*: 2014-11-03 |
Sponsor Name:AZIENDA PROVINCIALE PER I SERVIZI SANITARI DELLA PROVINCIA AUTONOMA DI TRENTO | ||
Full Title: CRANIAL-FACIAL PAIN TREATMENT: PROSPECTIC, RANDOMIZED, OPEN-LABEL STUDY ON TRANSNASAL NONSURGICAL BLOCKADE VERSUS PHARMACOLOGICAL THERAPY | ||
Medical condition: Cranial facial pain | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2014-005269-66 | Sponsor Protocol Number: BAYH6689/13130 | Start Date*: 2015-02-09 | |||||||||||
Sponsor Name:Bayer HealthCare AG | |||||||||||||
Full Title: A Multicenter, Double-Blind, Randomized, Parallel, Placebo-Controlled Trial Assessing the Analgesic Efficacy of a Single, Oral Dose of an Extended Release Naproxen Sodium Tablet in Postsurgical Den... | |||||||||||||
Medical condition: Toothache | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-002436-31 | Sponsor Protocol Number: ALGIPED | Start Date*: 2023-05-16 | |||||||||||
Sponsor Name:Dicofarm S.p.A. | |||||||||||||
Full Title: Randomized, controlled, transversal phase IV study on the efficacy and speed of action of lysin ibuprofen vs ibuprofen on the treatment of acute pain in children (ALGIPED). | |||||||||||||
Medical condition: Acute pain in pediatric age | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Not Authorised) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-002220-37 | Sponsor Protocol Number: UP-CLI-2020-001 | Start Date*: 2021-02-24 |
Sponsor Name:UNITHER Pharmaceuticals | ||
Full Title: Comparison of the analgesic effect of a new paracetamol formulation (paracetamol UNIFLASH) for buccal use and two different doses of an oral paracetamol form controlled versus placebo in patients s... | ||
Medical condition: Symptomatic short-term treatment of moderate pain | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) IT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2010-022798-32 | Sponsor Protocol Number: DEX-TRA 02 | Start Date*: 2010-12-14 | |||||||||||
Sponsor Name:Menarini Ricerche S.p.A. | |||||||||||||
Full Title: DOUBLE-BLIND, RANDOMISED, PLACEBO AND ACTIVE CONTROLLED, PARALLEL GROUP STUDY TO EVALUATE THE ANALGESIC EFFECT OF A SINGLE ORAL ADMINISTRATION OF FOUR DIFFERENT COMBINATION DOSES OF DKP.TRIS WITH T... | |||||||||||||
Medical condition: Severe pain following impacted third mandibular molar tooth extraction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) ES (Completed) HU (Completed) IT (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
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